Goto S, Nagahiro S, Korematsu K, Kogo K, Ushio Y
Department of Neurosurgery, Kumamoto University Medical School, Japan.
Acta Neuropathol. 1994;87(2):211-6. doi: 10.1007/BF00296192.
Behavioral and histological studies were performed on a reversible ischemia model in rats. At 60 days after unilateral transient middle cerebral artery occlusion for 30 min, the operated rats exhibited the ipsiversive rotational behavior elicited by systemic administration of dopamine receptor agonist apomorphine in a dose-dependent manner. Histologically, the ipsilateral striatum of the rats showed a subdivisional ischemic injury, while the nigral dopaminergic neurons appeared intact. The striatal lesions having a cell type-specific injury were located in the dorsolateral portion of the rostral striatum and in the lateral portion of the caudal part of the nucleus. Thus, the transient cerebral ischemia could successfully produce selective damage of a striatal subdivision, which causes an abnormality in motor controls in response to dopamine receptor stimulation. The present data may provide a part of functional and anatomical basis for understanding the movement disorders associated with basal ganglia dysfunction (e.g., parkinsonism), which may occur in patients with cerebrovascular disorders.
对大鼠可逆性缺血模型进行了行为学和组织学研究。在单侧大脑中动脉短暂闭塞30分钟后60天,手术大鼠表现出全身给予多巴胺受体激动剂阿扑吗啡所诱发的向患侧旋转行为,且呈剂量依赖性。组织学上,大鼠患侧纹状体显示出分区性缺血损伤,而黑质多巴胺能神经元似乎完好无损。具有细胞类型特异性损伤的纹状体病变位于尾状核头端背外侧部分和尾端外侧部分。因此,短暂性脑缺血能够成功地导致纹状体一个分区的选择性损伤,这会引起对多巴胺受体刺激的运动控制异常。本研究数据可能为理解与基底神经节功能障碍(如帕金森症)相关的运动障碍提供部分功能和解剖学基础,这些运动障碍可能发生在脑血管疾病患者中。